Canonical Allele Identifier: CA2248965592

Gene: COX10

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.14076912A= , CM000679.2:g.14076912A=	GRCh38
NC_000017.10:g.13980229A= , CM000679.1:g.13980229A=	GRCh37
NC_000017.9:g.13920954A=	NCBI36
NG_008034.1:g.12511A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261643.8:c.355A= MANE Select	ENSP00000261643.3:p.Ile119=
ENST00000664217.1:c.355A=	ENSP00000499396.1:p.Ile119=
ENST00000670279.1:c.355A=	ENSP00000499450.1:p.Ile119=
ENST00000261643.7:c.355A=	ENSP00000261643.3:p.Ile119=
ENST00000429152.6:c.355A=	ENSP00000397750.2:p.Ile119=
ENST00000580561.1:c.177+2456A=	ENSP00000462190.1:n.177+2456A=
ENST00000581931.5:c.355A=	ENSP00000462512.1:p.Ile119=
NM_001303.3:c.355A=	NP_001294.2:p.Ile119=
XM_005256458.1:c.355A=	XP_005256515.1:p.Ile119=
XM_011523657.1:c.355A=	XP_011521959.1:p.Ile119=
XM_011523658.1:c.-97A=	XP_011521960.1:n.-97A=
XR_933974.1:n.458A=
XR_933975.1:n.458A=
NM_001303.4:c.355A= MANE Select	NP_001294.2:p.Ile119=